The weekly research round-up now includes recent publications about ME/CFS […]
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
The new NICE Clinical Guideline for ME/CFS will be published on 18
Open Letters to Healthcare Professionals from people with ME/CFS – Part 5 Maryjane Read More »
The new NICE Clinical Guideline for ME/CFS will be published on 18
On Sunday 20th June for 12 hours, from 9am to
On Sunday 20th June for 12 hours, from 9am to
Following a disappointing article from Josh Glancy that appeared in
Following a disappointing article from Josh Glancy that appeared in
Members of the ME Association receive the quarterly magazine –
Members of the ME Association receive the quarterly magazine –
It was Carers week last week and we don’t often
It was Carers week last week and we don’t often
Scientists are starting to get insights into the lingering disorder
Nature Article: The four most urgent questions about long COVID Read More »
Scientists are starting to get insights into the lingering disorder
The weekly research round-up now includes recent publications about ME/CFS
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
Earlier this year I attended a medical webinar where we
Dr Shepherd on Treating Long Covid with Histamine Receptor Antagonists Read More »
Earlier this year I attended a medical webinar where we
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multi-system disease with a significant impact on the quality of life of patients and their families, yet the majority of ME/CFS patients go unrecognised or undiagnosed.
Research: Medical School Education on Myalgic Encephalomyelitis by Dr Nina Muirhead Read More »
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multi-system disease with a significant impact on the quality of life of patients and their families, yet the majority of ME/CFS patients go unrecognised or undiagnosed.
